A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509599



Internal ID20882910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96755201..96760600hg38UCSC Ensembl
chr15:97298431..97303830hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509599
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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